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Analysis of a grading system to assess the quality of small-bowel preparation for capsule endoscopy: in search of the Holy Grail

机译:分析用于评估胶囊内窥镜小瓶制剂质量的分级系统:寻找圣杯

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Background: The diagnostic yield of capsule endoscopy is vulnerable to inadequate visualization related to residual bile or chyme remaining in the lumen despite intestinal lavage. It has been challenging to determine the optimal lavage preparation of the bowel and patient diet before capsule endoscopy, as well as the timing of the procedure, because no well-accepted, validated grading system for assessing the quality of intestinal lavage before capsule endoscopy is available. There remains no consensus on the reliability of qualitative, quantitative, or computer-derived assessments of the quality of preparation for capsule endoscopy. This study evaluates intra-observer and interobserver agreement for a previously validated scale. Materials and methods: The digital images of 34 patients who underwent capsule endoscopy were independently reviewed by two blinded physicians according to a previously validated grading scale. One of the physicians reviewed and graded the patients a second time. The quality of the bowel luminal preparation was assessed with a qualitative parameter (fluid transparency) and a more quantitative parameter (mucosal invisibility) for each of three small-intestinal segments, and an overall small-bowel score for each parameter was assigned as well. A weighted kappa coefficient was used to calculate intra-observer (observer 1A and 1B) and interobserver (observer 1A and observer 2) agreement. A kappa value of 0.60 or more suggests strong agreement, 0.40 to 0.60 moderate agreement, and less than 0.40 poor agreement. Results: The intra-observer weighted kappa index for both fluid transparency and mucosal visibility was 0.52, which is consistent with moderate agreement. The interobserver weighted kappa indices for fluid transparency and mucosal invisibility were 0.29 and 0.42, respectively, demonstrating suboptimal interobserver agreement. The individual segment interobserver kappa indices were better for mucosal visibility (0.52, 0.39, and 0.47 for small-bowel segments 1, 2, and 3, respectively) than for fluid transparency (0.18, 0.38, and 0.31). Conclusions: The proposed grading scale for assessing the quality of preparation for capsule endoscopy has inadequate interobserver and intra-observer agreement. Capsule endoscopy preparation grading scales that focus more on quantitative than on qualitative assessment may demonstrate more reliable performance characteristics. Optimizing the quality of preparation and diagnostic yield of capsule endoscopy will first require the development of a well-validated grading scale.
机译:背景:胶囊内窥镜检查的诊断结果很容易因肠腔冲洗而残留在管腔内的残留胆汁或食糜相关的可视化不足。在胶囊内窥镜检查之前确定肠道和患者饮食的最佳灌洗准备以及手术时机是一项挑战,因为在胶囊内窥镜检查之前尚无公认的评估肠道灌洗质量的分级系统。关于胶囊内窥镜检查准备质量的定性,定量或计算机评估的可靠性尚无共识。这项研究评估了观察者之间和观察者之间的协议是否具有先前验证的规模。材料和方法:两名盲人医师根据先前验证的分级量表对34例接受胶囊内镜检查的患者的数字图像进行了独立检查。一位医师对患者进行了第二次检查和评分。通过三个小肠段中的每个肠段的定性参数(流体透明度)和更定量的参数(粘膜不可见性)评估肠腔准备的质量,并且还为每个参数指定了总体小肠评分。加权卡伯系数用于计算观察者内部(观察者1A和1B)和观察者之间(观察者1A和观察者2)的一致性。 kappa值等于或大于0.60时,表示一致性较高;表示一致性介于0.40到0.60之间;差值小于0.40。结果:观察者内部加权Kappa指数对液体透明度和粘膜可见性均为0.52,与中度一致性一致。观察者间加权的kappa指数表示液体透明性和粘膜不可见性,分别为0.29和0.42,这表明观察者间的一致性欠佳。观察者的各个节段间kappa指数对粘膜可见性更好(小肠节1、2和3分别为0.52、0.39和0.47),而不是流体透明性(0.18、0.38和0.31)。结论:拟议的用于评估胶囊内窥镜检查制剂质量的分级量表在观察者之间和观察者内部协议不足。胶囊内窥镜制剂的分级量表更侧重于定量而不是定性评估,可能显示出更可靠的性能特征。首先,要优化胶囊内窥镜的制备质量和诊断产率,首先需要开发一种经过充分验证的分级量表。

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